drugset / Trial / NCT05708274

Pharmacological Agents for Chronic Spinal Cord Injury (SCI)

NCT05708274

Phase 1 Completed 25 enrolled Bronx VA Medical Center
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to investigate the short-term effects of 3 approved FDA drugs (cyproheptadine (CPH), carbidopa-levodopa (CD-LD), and atomoxetine (ATX)) on motor responses when delivered in combination with hand training exercises in people with chronic spinal cord injury. The goal is to learn how to better strengthen connections between the brain and spinal cord after spinal cord injury, and if this connection is improved by one(or more) of the drugs. Multiple aspects of nerve transmission and muscle response will be measured via noninvasive brain and spinal cord stimulation, along with motor performance (dexterity and strength).

Timeline

Start
2023-01-20
Primary completion
2025-10-30
Completion
2025-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified 40 mg Oral
Subject Carbidopa Unknown 50 mg Oral
Subject Cyproheptadine Small molecule 8 mg Oral
Subject Levodopa Small molecule 200 mg Oral

Indications